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L-Leucine, N-[(2S,3R)-2-hydroxy-1-oxo-3-[[(phenylmethoxy)carbonyl]amino]octyl]-, phenylmethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

184652-45-7

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184652-45-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 184652-45-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,4,6,5 and 2 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 184652-45:
(8*1)+(7*8)+(6*4)+(5*6)+(4*5)+(3*2)+(2*4)+(1*5)=157
157 % 10 = 7
So 184652-45-7 is a valid CAS Registry Number.

184652-45-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name (2S,3R)-3-benzyloxycarbonylamino-2-hydroxyoctanoyl-L-leucine benzyl ester

1.2 Other means of identification

Product number -
Other names (S)-2-((2S,3R)-3-Benzyloxycarbonylamino-2-hydroxy-octanoylamino)-4-methyl-pentanoic acid benzyl ester

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:184652-45-7 SDS

184652-45-7Downstream Products

184652-45-7Relevant academic research and scientific papers

Stereospecific synthesis of a novel farnesyl protein transferase inhibitor, valinoctin A and its analogues

Tsuda, Makoto,Muraoka, Yasuhiko,Takeuchi, Tomio,Sekizawa, Ryuichi,Umezawa, Kazuo

, p. 1031 - 1035 (2007/10/03)

(2S,3R)-3-Amino-2-hydroxyoctanoic acid was synthesized by Curtius rearrangement of an azide derivative of (S)-malic acid. Total syntheses of valinoctin A and its analogues were achieved by a coupling of (2S,3R)-3-amino-2-hydroxyoctanoic acid moiety with L-valine or several other amino acids moieties. 2S configuration of 3-amino-2-hydroxyoctanoic acid moiety was found to be important for the inhibitory activity and the L-valine moiety of valinoctin A was exchangeable with other L-amino acids.

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